Mild cognitive impairment and Alzheimer patients display different levels of redox-active CSF iron
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Lavados Montes, Manuel
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Mild cognitive impairment and Alzheimer patients display different levels of redox-active CSF iron
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Abstract
Oxidative stress constitutes a hallmark of Alzheimer’s disease (AD). Recent studies also point to redox active metals
such as iron, copper and zinc in mediating oxidative stress in AD pathogenesis. However, the reactivity of cerebrospinal fluid
(CSF) iron and its possible correlation with the severity of cognitive decline in both Alzheimer’s patients and subjects with mild
cognitive impairment (MCI) is still unknown. Here we show that different stages of cognitive and functional impairment are
associated with changes in CSF reactive iron. In this work, we compared CSF samples from 56 elders, classified into 4 groups
according to their scores on the Clinical Dementia Rating scale (CDR). Total CSF iron was analyzed by atomic absorption
spectrometry. Redox-active iron was analyzed by a novel fluorimetric assay. One-way ANOVA was used to test differences in
mean values, and Newman-Keuls Multiple Comparison Test was used for multi group comparisons. No difference in total CSF
iron was found between different groups. Significant amounts of redox-active iron were found in CSF and their levels correlated
with the extent of cognitive impairment. Redox-active CSF iron levels increased with the degree of cognitive impairment from
normal to MCI subjects, while AD patients showed an abrupt decrease to levels close to zero.
Given the relevance of oxidative damage in neurodegeneration, it might be possible to associate the development of cognitive and
functional decline with the presence of redox-active iron in the CSF. The decrease in redox-active iron found in AD patients may
represent a terminal situation, whereby the central nervous system attempts to minimize iron-associated toxicity.
Patrocinador
This work was supported by the Millennium Institute
for Advanced Studies (CBB), the International Center
for Biomedicine (ICC) and FONDECYT projects
1050198 (to RBM) and 1010191 (to ML). JTE was
supported by MECESUP and CONICYT fellowships
from the PhD program in Pharmacology, Universidad
de Chile, and by The European Community 5th Framework
QLRT-2001-00444 (Nutrient iron toxicity).
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JOURNAL OF ALZHEIMERS DISEASE, Volume: 13, Issue: 2, Pages: 225-232, 2008
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